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Integrating a Mental Health Intervention Into Primary Health Care for Refugees

I

International Rescue Committee

Status

Enrolling

Conditions

Hypertension
Self Efficacy
Diabetes
Epilepsy
Medication Adherence
Mental Health Issue

Treatments

Behavioral: Common Elements Treatment Approach

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The objective of this study is to evaluate the impact of an evidence-based mental health intervention (Common Elements Treatment Approach) on medication adherence, behavioral improvement and clinical outcomesamong adults taking medication for hypertension, diabetes and epilepsy using a two-arm randomized wait-list controlled trial among adult refugees in Mae La camp, Thailand.

Enrollment

308 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • A. Inclusion criteria:

    1. Patients who was diagnosed by physician based on ICD 10 to have diabetes, hypertension or diabetes with hypertension comorbidity, or epilepsy.
    2. Registered in chronic database system of the camp.

B. Exclusion criteria:

  1. who are younger than 18 years old
  2. who have severe physical illness
  3. who have severe mental disorders
  4. who will not stay in the camp until the end of the program
  5. who are not willing to participate in the program

Exclusion criteria

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

308 participants in 2 patient groups

Intervention Arm
Experimental group
Description:
The course of Common Elements Treatment Approach (CETA - the intervention under study) is built to be flexible depending on need. Mild symptoms could result in fewer sessions (e.g., 5), while greater severity may require 8-12 sessions.
Treatment:
Behavioral: Common Elements Treatment Approach
Waitlisted Arm
No Intervention group
Description:
The waitlisted arm will be offered the CETA approach upon conclusion of the endline data collection.

Trial contacts and locations

1

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Central trial contact

Kathryn Falb; Ye Htut Oo

Data sourced from clinicaltrials.gov

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